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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252738Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 86620415, compound

https://huagongshe.com/reaction/252738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantLithium bis(trimethylsilyl)amideHCID 57426343—
ReactantHCID 86244451HCID 86244451—
CatalystWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86620415HCID 86620415—

Reaction Conditions

Temperature0 °C

Reaction Steps

Lithium hexamethyldisilazane (1M solution in THF; 0.81 mL) was added to a mixture of N-[5-(5-amino-6-chloropyridazin-3-yl)-4-methyl-1,3-thiazol-2-yl]acetamide (77 mg) and THF (1.3 mL) that had been cooled to 0° C. The reaction mixture was allowed to warm and was stirred at room temperature for 30 minutes. Benzenesulfonyl chloride (0.069 mL) was added and the reaction mixture was stirred at room temperature for 2 hours. Water (2 drops) was added to the reaction mixture. The mixture was evaporated and the residual solid was purified by preparative HPLC. The material so obtained was purified further by column chromatography on silica using a solvent gradient of 0% to 20% methanol in dichloromethane as eluent. There was thus obtained the title compound as a solid (2.5 mg); 1H NMR Spectrum: (DMSOd6) 2.15 (s, 3H), 2.40 (s, 3H), 7.05 (s, 1H), 7.45 (m, 3H), 7.80 (m, 2H); Mass Spectrum: M+H+ 424.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868188B2
Source datasetuspto-grants-2011_01
ORD IDord-e17a838fe86944ac96de3f340fb579c0
Source noteuspto-grants-2011_01